Synthesis of 2-hydroxy-5(3-methylcyclohexyl)aceto- and benzophenones in the presence of a nano-catalytic system

G. Haydarli, Ch. K. Rasulov, N. M. Alieva
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Abstract

The results of studying of the cycloalkylation reaction of phenol with 3-methylcyclohexene in the presence of zeolite Y impregnated with phosphoric acid are presented. It was found that in order to achieve a high yield (71.2%) and selectivity (93.7%) during the cycloalkylation reaction of phenol with 3-methylcyclohexene, the reaction conditions should be as follows: reaction temperature 120 oC, molar ratio of phenol to 3-methylcyclohexene 1:1, volume velocity 0.5 h-1. The results of the synthesis of 2-hydroxy-5(3-methylcyclohexyl) aceto- and benzophenones by the reaction of p-(3-methylcyclohexyl) phenol with acetic acid (AcOH) and benzoyl chloride (BzCl) with the participation of nanosized ZnCl2 as a catalyst are presented. It was found that at a temperature of 140 oC, a reaction time of 40 minutes, and a molar ratio of p-(3-methylcyclohexyl) phenol to AcOH (BzCl) of 1:2, the yield of the target products was 63.3-66.7%.
在纳米催化体系下合成2-羟基-5(3-甲基环己基)乙酰和二苯甲酮
介绍了在磷酸浸渍Y型沸石存在下苯酚与3-甲基环己烯环烷基化反应的研究结果。结果表明,苯酚与3-甲基环己烯的环烷基化反应,为获得较高的收率(71.2%)和选择性(93.7%),反应条件应为:反应温度120℃,苯酚与3-甲基环己烯的摩尔比1:1,体积速度0.5 h-1。介绍了在纳米ZnCl2催化下,对(3-甲基环己基)苯酚与乙酸(AcOH)和苯甲酰氯(BzCl)反应合成2-羟基-5(3-甲基环己基)乙酰和二苯甲酮的研究结果。结果表明,在温度为140℃、反应时间为40 min、对-(3-甲基环己基)苯酚与AcOH (BzCl)的摩尔比为1:2的条件下,目标产物的收率为63.3 ~ 66.7%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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